ライフサイエンスコーパス: multiphoton microscopy

1 vapour deposited monolayer MoS2 samples with multiphoton microscopy.

2 n imaging techniques, including confocal and multiphoton microscopy.

3 its, by far the largest of any label used in multiphoton microscopy.

4 he focal point specificity characteristic of multiphoton microscopy.

5 in CD were evaluated with flow cytometry and multiphoton microscopy.

6 This result was further confirmed with multiphoton microscopy.

7 olecules with deeper tissue penetration than multiphoton microscopy.

8 time to expected ovulation using intravital multiphoton microscopy.

9 r optical properties of few-layer GaSe using multiphoton microscopy.

10 when measured using intravital quantitative multiphoton microscopy.

11 uorescently labelled ipRGCs visualized using multiphoton microscopy.

12 nd closure up to 6 hours by autofluorescence multiphoton microscopy.

13 onitored plaque formation in real time using multiphoton microscopy.

14 e regulatory co-factor 2 (NHERF2-/- mice) by multiphoton microscopy.

15 extrans, assessed by intravital quantitative multiphoton microscopy.

16 and processes per cell visualized in vivo by multiphoton microscopy.

17 l orders of magnitude lower than traditional multiphoton microscopies.

18 Multiphoton microscopy allows for deep tissue penetratio

19 d at depths beyond the reach of conventional multiphoton microscopy and adaptive optics methods, albe

20 Parallel studies using multiphoton microscopy and in vivo microdialysis reveale

21 We used multiphoton microscopy and longitudinal imaging to monit

22 Using complementary multiphoton microscopy and quantitative analyses in wild

23 Multiphoton microscopy and scanning electron microscopy

24 ative brain tissues and in cultures by using multiphoton microscopy and second-harmonic generation fr

25 By combining multiphoton microscopy and sequencing, we show that tens

26 the recent preclinical insights gained using multiphoton microscopy and suggests future advances that

27 By incorporating multiphoton microscopy and the dsLNA biosensor, we perfo

28 A combination of multiphoton microscopy and voltage-clamp recording was u

29 e macula densa plaque using four-dimensional multiphoton microscopy and wide-field fluorescence micro

30 hat circumvents the technical limitations of multiphoton microscopy and, as a result, provides unprec

31 r scanning modalities including confocal and multiphoton microscopy, and offers artifact free reconst

32 The diameter of vessels was assessed with multiphoton microscopy, and the amount of renal collagen

33 nce laser techniques, including confocal and multiphoton microscopy, are opening new avenues for cell

34 image-guided therapeutic interventions, and multiphoton microscopy as the appropriate method of vali

35 tumor cell motility in the primary tumor by multiphoton microscopy, as well as a dramatically reduce

36 gical readouts, and sophisticated intravital multiphoton microscopy-based imaging of liver in mice.

37 Here, we demonstrate that multiphoton microscopy can be used to visualize the micr

38 Intravital multiphoton microscopy data show that sunitinib induces

39 Multiphoton microscopy enables imaging deep into scatter

40 Multiphoton microscopy enables live imaging of the renal

41 als (quantum dots) as fluorescent labels for multiphoton microscopy enables multicolor imaging in dem

42 Multiphoton microscopy facilitated repeated imaging deep

43 Using a combination of intravital multiphoton microscopy, genetically modified mice and no

44 Although intravital multiphoton microscopy has addressed this limitation, th

45 veral years, in vivo imaging of tumors using multiphoton microscopy has emerged as a powerful preclin

46 Multiphoton microscopy has enabled unprecedented dynamic

47 Intravital multiphoton microscopy has provided powerful mechanistic

48 re and exogenous contrast agents that enable multiphoton microscopy, however, limit the ability to in

49 features are confirmed by coregistration of multiphoton microscopy images with conventional histolog

50 Here we report that multiphoton microscopy imaging of polytene nuclei in liv

51 in vivo, we observed cortical neurons using multiphoton microscopy in a mouse model of amyloid patho

52 Multiphoton microscopy in acute hippocampal slices confi

53 of tubular cell structure and function with multiphoton microscopy in an intact, functioning organ.

54 Using multiphoton microscopy in live cells, we show that free

55 ate cells (PSC) in culture and in situ using multiphoton microscopy in pancreatic lobules.

56 Overall, these data suggest that multiphoton microscopy is a highly sensitive and promisi

57 Multiphoton microscopy is a powerful tool in neuroscienc

58 Multiphoton microscopy is the current method of choice f

59 In vivo, multiphoton microscopy is used to image through an intac

60 Here, we have used in vivo multiphoton microscopy, laser speckle imaging of CBF, an

61 Multiphoton microscopy (MPM) has found a niche in the wo

62 Multiphoton microscopy (MPM) holds promise as a noninvas

63 We analyzed multiphoton microscopy (MPM) images corresponding to 15

64 Multiphoton microscopy (MPM) is a nonlinear fluorescence

65 Here we report the development of serial multiphoton microscopy (MPM) of the same glomeruli over

66 Recent translation of multiphoton microscopy (MPM) to clinical practice raises

67 h signals, we used high-resolution live-cell multiphoton microscopy (MPM) to directly observe cellula

68 e we developed an imaging approach that uses multiphoton microscopy (MPM) to directly visualize podoc

69 By applying the new technique of multiphoton microscopy (MPM) with clearing to a new mous

70 As evidenced by intravital multiphoton microscopy of Ccr2 reporter mice, CCR2(+) mo

71 Multiphoton microscopy of collagen hydrogels produces se

72 Using longitudinal intravital multiphoton microscopy of DC(GFP)/MC(RFP) reporter mice,

73 Long-term time-lapse multiphoton microscopy of embryonic mouse cortex reveals

74 Multiphoton microscopy of embryos produced by these worm

75 Here, we show how multiphoton microscopy of fluorescently tagged BDNF in b

76 ntitate dendritic protein synthesis, we used multiphoton microscopy of green fluorescent protein synt

77 Multiphoton microscopy of kidney sections confirmed that

78 We have used time-lapse multiphoton microscopy of living Tg(fli1:EGFP)y1 zebrafi

79 By high-resolution multiphoton microscopy of mammary carcinoma in mice, we

80 al procedure suitable for time-lapse in vivo multiphoton microscopy of mouse spinal cord without the

81 tion multiplex static imaging and intravital multiphoton microscopy of Mycobacterium bovis BCG-induce

82 Intravital multiphoton microscopy of potential-indicating rhodamine

83 l death were assessed by intravital confocal/multiphoton microscopy of rhodamine 123 (Rh123) and prop

84 and MPT were detected by intravital confocal/multiphoton microscopy of rhodamine 123, propidium iodid

85 We employed in vivo multiphoton microscopy of the genetically encoded Ca(2+)

86 This study demonstrates that multiphoton microscopy of the isolated perfused kidney i

87 RECENT FINDINGS: Imaging modalities like multiphoton microscopy, optical coherence tomography, Co

88 oscopy over relatively short periods, and by multiphoton microscopy over more extended periods that i

89 Using multiphoton microscopy, Pittsburgh compound B (PIB) was

90 Multiphoton microscopy relies on nonlinear light-matter

91 Multiphoton microscopy revealed more efficient interacti

92 After induction of inflammation, multiphoton microscopy revealed that approximately 20% o

93 Moreover, intravital multiphoton microscopy revealed that Debio0719 reduced t

94 Resonant-scanning multiphoton microscopy revealed that in vivo arterial st

95 Confocal and multiphoton microscopy revealed that the paleness of lcd

96 Multiphoton microscopy reveals that intercalating cells

97 Intravital multiphoton microscopy reveals that Stat3 silencing comb

98 Here, multiphoton microscopy reveals the direct transformation

99 aging over 3D volumes in living retina using multiphoton microscopy should now allow fundamental mech

100 the imaging of the skin hair follicles using multiphoton microscopy showed that it opened the follicu

101 nte Carlo-based radiative transport model of multiphoton microscopy signal collection in skin, establ

102 Most multiphoton microscopy studies in biological systems hav

103 in probe choice and experimental design for multiphoton microscopy studies.

104 Here, we used multiphoton microscopy techniques and transgenic mice th

105 t parasites combined with flow cytometry and multiphoton microscopy techniques to understand the even

106 dvantage of recent technological advances in multiphoton microscopy that have allowed its application

107 rm and methodology for label-free multimodal multiphoton microscopy that uses a novel photonic crysta

108 We now show, using in vivo multiphoton microscopy, that FITC-labeled F(ab')2 fragme

109 Using serial intravital multiphoton microscopy through a thinned-skull cranial w

110 ion and progression of CAA in Tg2576 mice by multiphoton microscopy through cranial windows.

111 We used QDs and emission spectrum scanning multiphoton microscopy to develop a means to study extra

112 hods ranging from fluorescence, confocal and multiphoton microscopy to electron microscopic imaging a

113 The mixer is used in conjunction with multiphoton microscopy to examine the fast Ca2+-induced

114 We have combined this model with multiphoton microscopy to image differences in cell beha

115 The efficient application of multiphoton microscopy to intrinsic imaging requires kno

116 Herein, we used in vivo multiphoton microscopy to investigate NET formation in t

117 We have used time-lapse multiphoton microscopy to map the migration and settling

118 ident microglia in living mice and then used multiphoton microscopy to monitor these cells over time.

119 Here, we use multiphoton microscopy to obtain quantitative data of el

120 Here, we employed nonlinear multiphoton microscopy to quantify collagen fiber organi

121 We utilized multiphoton microscopy to quantify the dynamic behavior

122 c architecture, we used longitudinal in vivo multiphoton microscopy to sequentially image young APPsw

123 issue of Cell, Langen et al. use time-lapse multiphoton microscopy to show how Drosophila photorecep

124 Here we use brain slice multiphoton microscopy to show that substantia nigra dop

125 In this study, we use multiphoton microscopy to show, for the first time, that

126 With increasing applications of multiphoton microscopy to thick-tissue "intravital" imag

127 To address this, we used intravital multiphoton microscopy to visualize immune cell interact

128 Here we used multiphoton microscopy to visualize the dynamics and act

129 Using in vivo multiphoton microscopy together with fluorescently label

130 Multiphoton microscopy utilizing second harmonic generat

131 By using multiphoton microscopy, Voxx software, and the Tie-2 mou

132 In vivo time-lapse multiphoton microscopy was used to analyze the remodelin

133 METHODS AND Multiphoton microscopy was used to image deep within car

134 Multiphoton microscopy was used to image renal dendritic

135 Using transcranial in vivo multiphoton microscopy, we find that fmr1 KO mice have s

136 Using multiphoton microscopy, we found five major differences

137 Using intravital multiphoton microscopy, we measured presynaptic activity

138 Using multiphoton microscopy, we observed and monitored amyloi

139 Using conditional mutants and intravital multiphoton microscopy, we show here that the lipid medi

140 Using in vivo multiphoton microscopy, we show that morpholino-mediated

141 Using multiphoton microscopy, we show that, in vivo, CD11c(+)

142 Further, using multiphoton microscopy, we show the utility of this tool

143 ly used imaging methods such as confocal and multiphoton microscopy, when combined with techniques su

144 al imaging systems that combine confocal and multiphoton microscopy with inertia-free laser scanning.